Myanmar FDA registration fa9c797800c5ee749019739cbf090803

Light Source

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Coroporation Hanamaki Office·Registered September 27, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: fa9c797800c5ee749019739cbf090803
Registration Date: September 27, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Coroporation Hanamaki Office

Authorized Representative

Name: SNOW EVEREST COMPANY LIMITED

About this record

Access comprehensive regulatory information for Light Source in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fa9c797800c5ee749019739cbf090803 and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Hanamaki Office. The device was registered on September 27, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.